Alzheimer's disease (AD) is a debilitating disease for which there is no current cure, which worsens as it progresses, eventually leading to death. Currently there are no generally acceptable biomarkers for AD, and the diagnosis of this condition, while improved, is generally subjective. Often such diagnoses are confirmed late in the disease progression, when damage to neural tissue has limited treatment options. The measurement of amyloid β protein (1-42), tau protein, and phosphorylated tau have been proposed as biomarkers measured in the cerebrospinal fluid (CSF) of symptomatic individuals. These, in conjunction with more sensitive imaging techniques involving the CSF introduction of dyes that target these same proteins, are able to identify some fraction of AD patients, but not at its earliest stage. These approaches are, however, invasive, expensive, and unfeasible as screening techniques.